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Changing the palladium coordination to phosphinoimidazolines with a remote triazole substituent
Adv. Synth. Catal. 2011, 353, 3255-3261.
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Continuous-flow enantioselective alpha-aminoxylation of aldehydes catalyzed by a polystyrene-immobilized hydroxyproline
Beilstein J. Org. Chem. 2011, 7, 1486-1493. -
Polystyrene-supported diarylprolinol ethers as highly efficient organocatalysts for Michael-type reactions
Chem. Eur. J. 2011, 17, 11585-11595.*This paper has been selected by the Editorial Board of SYNFACTS for its important insights: Synfacts 2011,12, 1375-1375
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Copper-free intramolecular alkyne-azide cycloadditions leading to seven-membered heterocycles
Org. Lett. 2011, 13, 5044-5047.
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Two distinct conformations of GABA locked by embedding in the bicyclo[3.1.0]hexane core structure
COVER ChemMedChem 2011, 6, 1792-1795.![Two distinct conformations of GABA locked by embedding in the bicyclo[3.1.0]hexane core structure](https://www.iciq.org/wp-content/uploads/2014/03/Two-distinct-conformations_1792.gif)
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A computational study on the role of chiral N-oxides in enantioselective Pauson–Khand reactions
Chem. Eur. J. 2011, 17, 10050-10057.
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Highly active organocatalysts for asymmetric anti-Mannich reactions
Chem. Eur. J. 2011, 17, 8780-8783.
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Polystyrene-supported enantiopure 1,2-diamines: Development of a most practical catalyst for the asymmetric transfer hydrogenation of ketones
Adv. Synth. Catal. 2011, 353, 1345-1352.
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Modular optimization of enantiopure epoxide-derived P,S-ligands for rhodium-catalyzed hydrogenation of dehydroamino acids
Tetrahedron 2011, 67, 4161-4168.
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Functionalization of Fe3O4 magnetic nanoparticles for organocatalytic Michael reactions
J. Mater. Chem. 2011, 21, 7350-7355.
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Catalytic batch and continuous flow production of highly enantioenriched cyclohexane derivatives with polymer-supported diarylprolinol silyl ethers
Synlett 2011, 464-468.
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Proline-derived aminotriazole ligands: Preparation and use in the ruthenium-catalyzed asymmetric transfer hydrogenation
Adv. Synth. Catal. 2011, 353, 113-124.*This paper has been selected by the Editorial Board of SYNFACTS for its important insights: Synfacts 2011, 4, 0408-0408
